chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101657514416575145TC27GENICpossibly homozygous615955488
101657532216575331GTCCTTCCA---------14GENIChomozygous736117106
101657540116575402AATT22GENICpossibly homozygous736117107
101657540116575402AATCTTT22GENICheterozygous736117108
101657561316575614AC17GENIChomozygous613978502
101657571616575717TTA21GENICpossibly homozygous736117109
101657587316575874AG20GENIChomozygous613978503
101657591016575911CT30GENIChomozygous613978504
101657602716576028A-15GENIChomozygous736117110
101657653716576538GGT21GENIChomozygous736117111